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A Manual of the Chemistry of the Carbon Compounds

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140 THE CHEMISTRY OF<br />

at 187°, and with water yields ethyl alcohol, acetone, and carbon<br />

dioxide.<br />

If <strong>the</strong> solid product obtained by <strong>the</strong> aotioa <strong>of</strong> sodium upon acetic<br />

e<strong>the</strong>r is acted upon by ethyl iodide, different compounds are formed,<br />

which can be separated by fractional distillation; amongst <strong>the</strong>m <strong>the</strong>re<br />

are e<strong>the</strong>rs <strong>of</strong> <strong>the</strong> fatty acids, such as ethyl-acetic acid or butyric acid,<br />

which is produced by <strong>the</strong> substitution <strong>of</strong> ethyl for one atom <strong>of</strong><br />

hydrogen in <strong>the</strong> methyl group <strong>of</strong> acetic aoid, <strong>the</strong> radical methyl being<br />

thus changed into propyl:—<br />

CHJtfa Q r ,<br />

I + C2H6I =| 4 Nal<br />

C0.0C$H6 CO.OC8H6<br />

In a similar way diethyl-aoetie acid, an isomeride <strong>of</strong> caproic acid,<br />

is obtained;—<br />

CHNa,<br />

+ 2C2H6I = I<br />

A0,0CaH6<br />

C0.0C2H6<br />

Ano<strong>the</strong>r class <strong>of</strong> compounds are formed by <strong>the</strong> action <strong>of</strong> ethyl<br />

iodide upon <strong>the</strong> sodacetone-carbonic e<strong>the</strong>rs:—<br />

CHS<br />

GO CO<br />

i.OC8H6<br />

CO.OC8HS<br />

Nal<br />

The ethyl ethacetone-carlonate thus fovmed is readily decomposed<br />

by baryta-water, <strong>the</strong> products being alcohol, barium, carbonate, and<br />

y y , p g<br />

methyl-propyl feetoue CO I „ tf.<br />

B By a similar iil reaction ti disoaacetone-carbanv: d i t<br />

e<strong>the</strong>r yields ethyl<br />

duthaeetoniHxirbonate, which is attacked by baryta-water in a similar<br />

•way as <strong>the</strong> preceding compound .-

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